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G6PC anticorps

L’anticorps Lapin Polyclonal anti-G6PC a été validé pour ELISA et IHC. Il convient pour détecter G6PC dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7245446

Aperçu rapide pour G6PC anticorps (ABIN7245446)

Antigène

Voir toutes G6PC Anticorps
G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))

Reactivité

  • 45
  • 22
  • 22
  • 16
  • 14
  • 13
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 46
  • 3
Lapin

Clonalité

  • 46
  • 3
Polyclonal

Conjugué

  • 17
  • 5
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp G6PC est non-conjugé

Application

  • 37
  • 20
  • 18
  • 11
  • 11
  • 6
  • 6
  • 4
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of human G6PC

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.44 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))

    Autre désignation

    G6PC

    Sujet

    Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.

    UniProt

    P35575

    Pathways

    Carbohydrate Homeostasis, Cellular Glucan Metabolic Process
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